11th Ed. Medical Device Safety Monitoring Reporting And Surveillance 2025

Descripción general

This conference will enable attendees to recognize and interpret future regulatory improvements and increase cooperation between member states in data collection, reporting, vigilance, and market surveillance. Attendees will continue education and deepen discussion revolved around coordinated efforts for validation of RWE collection, assessment of post market and clinical investigations and usage to ensure patient safety, health outcomes, and improved decision making.